Hydroxypropyl-β-cyclodextrin grafted polyethyleneimine used as transdermal penetration enhancer of diclofenac sodium

被引:26
|
作者
Yan, Yan [1 ]
Xing, Jianfeng [1 ]
Xu, Wei [1 ]
Zhao, Guilan [1 ]
Dong, Kai [1 ]
Zhang, Lu [1 ]
Wang, Ke [1 ]
机构
[1] Xi An Jiao Tong Univ, Hlth Sci Ctr, Sch Pharm, Xian 710061, Peoples R China
关键词
Transdermal drug delivery; Penetration enhancer; Diclofenac sodium; Cytotoxicity; Irritation of the skin; VITRO PERCUTANEOUS-ABSORPTION; IN-VITRO; TOPICAL DELIVERY; PERMEATION ENHANCERS; LIPID NANOPARTICLES; DRUG-DELIVERY; MICROEMULSION; PERMEABILITY; RELEASE; COMPLEX;
D O I
10.1016/j.ijpharm.2014.08.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The objective of this investigation was to develop a novel cationic polymer, hydroxypropyl-beta-cyclodextrin grafted polyethyleneimine (HP-beta-CD-PEI1800), as a penetration enhancer, and evaluate its viability on improving transdermal delivery of diclofenac sodium. In this study, HP-beta-CD-PEI1800 was characterized by 1H NMR and DSC methods, respectively. The hydrophilic drug diclofenac sodium was chosen as model drug, and the transdermal permeation enhancement of HP-beta-CD-PEI1800 was estimated in vitro by using Franz diffusion cells fitted with mouse dorsal skins, the in vivo kinetics of diclofenac sodium was analyzed by high performance liquid chromatography (HPLC). The cumulative drug content deposited in epidermis and dermis was measured at the pre-determined time point of 3, 6, and 9 h, and the permeation profile was significantly higher than that of the control groups. In addition, the cytotoxicity and skin irritation of enhancer was evaluated by MTT assay and histological examination, respectively, and the results indicated that the polymer we prepared were non-toxic and non-irritant after exposure to skins. All the results suggested that HP-beta-CD-PEI1800 could be a safe and efficient penetration enhancer of diclofenac sodium. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:182 / 192
页数:11
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